QC Associate ScientistA Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.This position is with my direct clientJob DescriptionResponsibilities:Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliancePerforms testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance.Responsible for final authorization/approval/release of documentation/equipment/processesAssessing existing situations and suggesting improvements in the Quality systems to increase compliance throughout the facilityPlans projects and may initiate and develop plans to ensure their timely completionQualificationsQualifications and Skills Needed:Work experience/skills: Minimum: 4 years of manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.Educational background: Minimum: BS/BA degree in Science/related field or other appropriate education/experience in biotech or pharmaceutical industryOR1-3 years of GMP experience.